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Variant : CV189151 (Single allele) Homo sapiens

Symbol: CV189151
Name: Single allele
Condition: not provided [RCV000171541]
Clinical Significance: likely pathogenic
Last Evaluated:
Review Status: classified by single submitter|criteria provided, single submitter
Related Genes: NHS  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh37X17,744,617 - 17,744,617CLINVAR
Cytogenetic MapXXp22.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 10045345
Created: 2015-06-09
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.